Antibodies specific to heterodimers of bcl-2 family and uses thereof

ABSTRACT

Isolated antibodies specifically binding to heterodimers of the Bcl-2 family and uses thereof for detecting presence of Bcl-2 heterodimers in a patient.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to U.S. provisional Patent ApplicationNo. 61/051,206, filed May 7, 2008, the content of which is incorporatedherein by reference in its entirety.

BACKGROUND OF THE INVENTION

Apoptosis is a process of programmed cell death mediated by a number ofsignaling pathways that converge at the mitochondria. A group ofmitochondrial proteins, i.e., the Bcl-2 proteins, regulates thisprocess. More specifically, pro-apoptotic and anti-apoptotic Bcl-2proteins form heterodimers with their cognate regulating Bcl-2 proteins(i.e., the BH3-only Bcl-2 proteins), thereby executing cell death orsurvival signals.

Essentially all effective cancer dugs induce apoptosis in target cancercells. However, different cancer cells respond to an apoptosis-inducingdrug in different manners. This is due to the presence of differentheterodimers between the pro/anti-apoptotic Bcl-2 proteins and theregulatory BH3-only Bcl-2 proteins in those cancer cells. Determiningthe presence of these heterodimers in a cancer patient helps assessingthat patient's responsiveness to an apoptosis-inducing cancer drug.

SUMMARY OF THE INVENTION

One aspect of this invention features an isolated antibody thatspecifically binds to a heterodimer of the Bcl-2 family (i.e., a Bcl-2heterodimer). The Bcl-2 family includes both Bcl-2 proteins (monomers)and naturally-occurring heterodimers formed between two Bcl-2 proteins.The heterodimer contains a first Bcl-2 protein (e.g., Bim, Bid, Bad,Puma, Noxa, Bak, Hrk, Bax, or Mule) and a second Bcl-2 protein (e.g.,Mcl-1, Bcl-2, Bel-XL, Bfl-1 or Bcl-w).

The antibody of this invention can be a monoclonal antibody, apolyclonal antibody, a chimeric antibody, or a humanized antibody. Italso can be a functional fragment of a whole antibody, such as F(ab′)₂,Fab′, F(ab)₂), and Fab. Alternatively, the antibody of this invention isa single chain antibody, e.g., a single chain variable fragment (scFv).

Another aspect of this invention is a method for detecting the presenceof a heterodimer of the Bcl-2 family using any of the antibodiesdescribed above. This method includes (i) providing a tissue samplesuspected of having a heterodimer of the Bcl-2 family, (ii) contactingthe sample with the antibody, (iii) detecting a signal indicative ofbinding of the antibody to the heterodimer, and (iv) determining thepresence of the heterodimer in the sample based on the intensity of thesignal. Examples of the heterodimer include Bim/Mcl-1 and Bim/Bcl-2. Thetissue sample examined in this method can be a peripheral blood sample,a lymph-node sample, a bond marrow sample, or an organ tissue sample.Preferably, it is a mitochondrial fraction.

Also within the scope of this invention is a method for assessingwhether a patient is sensitive or resistance to a drug that interfereswith formation of a heterodimer of the Bcl-2 family based on thepresence of that heterodimer in the patient. A cancer patient issensitive to an apoptosis inducer that blocks formation of ananti-apoptotic Bcl-2 heterodimer if this heterodimer is present in thatpatient. A neurodegenerative disease or cardiovascular disease patient,on the other hand, is responsive to an apoptosis inhibitor that blocksformation of a pro-apoptotic Bcl-2 heterodimer if this heterodimer ispresent in that patient.

The details of one or more examples of the invention are set forth inthe description below. Other features or advantages of the presentinvention will be apparent from the following drawings, detaileddescription of several examples, and also from the appended claims.

BRIEF DESCRIPTION OF THE DRAWINGS

The drawings are first described.

FIG. 1 is a schematic illustration depicting the conformational changeof a multidomain Bcl-2 protein induced by dimerization with a BH3-onlyBcl-2 protein.

FIG. 2 is a schematic illustration depicting the process of selectingantibodies specific to Bcl-2 heterodimers via an immunoassay. Panel A:antibodies binding to a Bcl-2 heterodimer being positively selected.Panel B: antibodies binding to non-dimerized members of the heterodimerbeing negatively selected. Panel C: illustration of what the symbols inPanels A and B represent.

FIG. 3 is a schematic illustration depicting an immunoassay forprofiling Bcl-2 heterodimers on mitochondria using the antibody of thisinvention, i.e., an antibody specifically recognizes Bcl-2 heterodimers,and an anti-VDAC antibody that recognizes mitochondria. Panel A:mitochondria presenting Bcl-2 heterodimers being recognized by both theantibody of this invention and an anti-VDAC antibody. Panel B:mitochondria not presenting Bcl-2 heterodimers being recognized by onlythe anti-VDAC antibody. Panel C: illustration of what the symbols inPanels A and B represent.

FIG. 4 is a schematic illustration showing identification of scFvantibodies specific to Bcl-2 heterodimers from a yeast display scFvlibrary.

FIG. 5 is a schematic illustration depicting a Luminex bead assay forprofiling Bcl-2 heterodimers in a patient sample. Panel A: multi-colorbeads used in the Luminex bead assay. Panel B: illustration of what thesymbols in Panels A and B represent.

DETAILED DESCRIPTION OF THE INVENTION

Disclosed herein is an isolated antibody specific to a Bcl-2heterodimer, i.e., a naturally-occurring heterodimer formed between twoBcl-2 proteins.

Bcl-2 proteins, found in mitochondria, are major regulators of thecommitment to programmed cell death and executioners of death/survivalsignals. See Reed, Natural Clinical Practice Oncology, 3:388-398 (2006),Green et al., Cancer Cell 1:19-30 (2002), and Adams et al., Cold SpringHarb. Symp. Quant. Biol. 70:469-477 (2005). There are four subgroups ofBcl-2 proteins: (i) multi-domain anti-apoptotic Bcl-2 proteins, (ii)multi-domain pro-apoptotic Bcl-2 proteins, (iii) activator BH3-onlyBcl-2 proteins, and (iv) sensitizer BH3-only Bcl-2 proteins. Table 1below lists major human Bcl-2 proteins and their GenBank accessionnumbers:

TABLE 1 Human Bcl-2 Proteins Bcl-2 Proteins GenBank Accession NumbersMulti-domain Bcl-2 AAH27258 (Jul. 15, 2006) Anti-Apoptotic Bcl-XLAAH19307 (Jul. 15, 2006) Bcl-2 Proteins Mcl-1 AAF64255 (Jul. 17, 2000)BCL-w AAB09055 (Sep. 29, 1996) BFL-1 Q16548 (Mar. 3, 2009) Multi-domainBAX Q07812 (Apr. 14, 2009) Pro-Apoptotic BAK Q16611 (Apr. 14, 2009)Bcl-2 Proteins Sensitizer BH3- BAD CAG46757 (Jun. 29, 2004) only Bcl-2BIK CAG30276 (Oct. 16, 2008) Proteins NOXA Q13794 (Mar. 3, 2009) HRKAAC34931 (Sep. 9, 1998) BMF AAH69328 (Aug. 19, 2004); AAH60783 (Jan. 27,2004) PUMA Q9BXH1 (Apr. 14, 2009) Mule Q7Z6Z7 (Apr. 14, 2009) ActivatorBH3- BID P55957 (Mar. 3, 2009) only Bcl-2 BIM O43521 (Apr. 14, 2009)ProteinsOther Bcl-2 proteins, if any, can be identified by homologous searchusing the amino acid sequence of a known Bcl-2 protein as a query.

It is known that members in one subgroup of Bcl-2 proteins formheterodimers with members in a different subgroup to regulate apoptosis.Formation of a heterodimer induces conformational changes in bothmembers of the heterodimer, resulting in exposure of antigenic epitopesthat are sequestered in both members before dimerization. See FIG. 1.The isolated antibody of this invention specifically recognizes such anepitope (e.g., the arrow epitope shown in FIG. 1). In other words, itonly binds to a heterodimer of the Bcl-2 family, not to eithernon-dimerized member.

This antibody can be a whole immunoglobulin or a fragment thereof thatretains antigen-binding activity. It can be a genetically modifiedimmunoglobulin, including scFv antibody, chimeric antibody, andhumanized antibody. The term “isolated antibody” used herein refers toan antibody substantially free from naturally associated molecules,i.e., the naturally associated molecules constituting at most 20% by dryweight of a preparation containing the antibody.

The antibody of this invention can be prepared by conventional methods.See, for example, Harlow and Lane, (1988) Antibodies: A LaboratoryManual, Cold Spring Harbor Laboratory, New York. In general, aheterodimer of the Bcl-2 family can be prepared by producing its twomembers separately by recombinant technology and then incubate bothmembers under suitable conditions to allow formation of the heterodimer.To produce antibodies against the heterodimer, the heterodimer,optionally coupled to a carrier protein (e.g., KLH) can be mixed with anadjuvant, and injected into a host animal. Antibodies produced in theanimal can then be purified by heterodimer affinity chromatography.Commonly employed host animals include rabbits, mice, guinea pigs, andrats. Various adjuvants that can be used to increase the immunologicalresponse depend on the host species and include Freund's adjuvant(complete and incomplete), mineral gels such as aluminum hydroxide, CpG,surface-active substances such as lysolecithin, pluronic polyols,polyanions, peptides, oil emulsions, keyhole limpet hemocyanin, anddinitrophenol. Useful human adjuvants include BCG (bacilleCalmette-Guerin) and Corynebacterium parvum. Polyclonal antibodies,i.e., heterogeneous populations of antibody molecules, are present inthe sera of the immunized animal.

Monoclonal antibodies, i.e., homogeneous populations of antibodymolecules, can be prepared using standard hybridoma technology (see, forexample, Kohler et al. (1975) Nature 256, 495; Kohler et al. (1976) Eur.J. Immunol. 6, 511; Kohler et al. (1976) Eur J Immunol 6, 292; andHammerling et al. (1981) Monoclonal Antibodies and T Cell Hybridomas,Elsevier, N.Y.). In particular, monoclonal antibodies can be obtained byany technique that provides for the production of antibody molecules bycontinuous cell lines in culture such as described in Kohler et al.(1975) Nature 256, 495 and U.S. Pat. No. 4,376,110; the human B-cellhybridoma technique (Kosbor et al. (1983) Immunol Today 4, 72; Cole etal. (1983) Proc. Natl. Acad. Sci. USA 80, 2026, and the EBV-hybridomatechnique (Cole et al. (1983) Monoclonal Antibodies and Cancer Therapy,Alan R. Liss, Inc., pp. 77-96). Such antibodies can be of anyimmunoglobulin class including IgG, IgM, IgE, IgA, IgD, and any subclassthereof. The hybridoma producing the monoclonal antibodies of theinvention may be cultivated in vitro or in vivo. The ability to producehigh titers of monoclonal antibodies in vivo makes it a particularlyuseful method of production.

In addition, techniques developed for the production of “chimericantibodies” can be used. See, e.g., Morrison et al. (1984) Proc. Natl.Acad. Sci. USA 81, 6851; Neuberger et al. (1984) Nature 312, 604; andTakeda et al. (1984) nature 314:452. A chimeric antibody is a moleculein which different portions are derived from different animal species,such as those having a variable region derived from a murine monoclonalantibody and a human immunoglobulin constant region. Alternatively,techniques described for the production of single chain antibodies (U.S.Pat. Nos. 4,946,778 and 4,704,692) can be adapted to produce a phage oryeast library of scFv antibodies. scFv antibodies are formed by linkingthe heavy and light chain fragments of the Fv region via an amino acidbridge.

Moreover, antibody fragments can be generated by known techniques. Forexample, such fragments include, but are not limited to, F(ab′)₂fragments that can be produced by pepsin digestion of an antibodymolecule, and Fab fragments that can be generated by reducing thedisulfide bridges of F(ab′)₂ fragments. Antibodies can also be humanizedby methods known in the art. For example, monoclonal antibodies with adesired binding specificity can be commercially humanized (Scotgene,Scotland; and Oxford Molecular, Palo Alto, Calif.). Fully humanantibodies, such as those expressed in transgenic animals are alsofeatures of the invention (see, e.g., Green et al. (1994) NatureGenetics 7, 13; and U.S. Pat. Nos. 5,545,806 and 5,569,825).

The antibodies prepared by any of the methods described above areconfirmed for their binding to a Bcl-2 heterodimer. They are furthersubjected to a negative selection to exclude those that also bind toeither non-dimerized member of the heterodimer. See FIG. 2. One examplefollows. Each of the two members, i.e., monomer A and monomer B, islabeled with a distinct fluorescent dye, i.e., dye x and dye y,respectively. Dyes x and y have different optimal emission wavelengths.The antibody is first incubated with labeled monomer A, labeled monomerB, or the A/B heterodimer (double labeled) for a suitable period andthen captured by GamaBind Sepharose beads. Whether the antibody iscapable of binding to either monomer or to the heterodimer can bedetermined based on the fluorescent signal released from the capturedantibody. Antibodies that bind to the heterodimer and not to eithernon-dimerized member are selected See FIG. 2.

The antibody of this invention can be used to detect the presence orabsence of a Bcl-2 heterodimer in a patient sample, particularly, afixed tissue sample or a mitochondrial fraction, by conventionalmethods, e.g., histochemistry staining. See FIG. 3. In one example, aplurality of antibodies specific to various Bcl-2 heterodimers are usedto profile the presence of particular Bcl-2 heterodimers on the outermembranes of mitochondria in multiple tissue samples from a patient.Tissues at various disease stages (e.g., malignancy stages) can becollected from the same patient. Mitochondrial fractions can be preparedfrom these tissues and, using a plurality of the antibodies of thisinvention, the fractions can be profiled for the presence/absence ofBcl-2 heterodimers.

Also disclosed herein is a method of predicting a human patient'sresponsiveness to a drug that interferes with formation of a particularBcl-2 heterodimer, directly or indirectly, based on the presence of thatBcl-2 heterodimer in the patient.

It well known that Bcl-2 proteins paly an essential role in regulatingapoptosis via formation of heterodimers between members in differentBcl-2 sub-groups. See Table 1 above. An activator BH3-only Bcl-2 protein(i.e., BID or BIM) binds to a multi-domain pro-apoptotic Bcl-2 protein(i.e., BAX or BAK), triggering mitochondrial outer membranepermeabilization (MOMP), which leads to cell death. A multi-domainanti-apoptotic Bcl-2 protein (e.g., Bcl-2 or Mcl-1) can bind to BAX andBAK, and also sequester an activator BH3-only protein from binding toBAX or BAK. Consequently, it blocks the MOMP process, resulting in cellsurvival. The activity of a multi-domain anti-apoptotic Bcl-2 protein isregulated by the sensitizer BH3-only proteins. This subgroup of Bcl-2proteins promotes apoptosis by binding to the anti-apoptotic Bcl-2protein, displacing the activator BH3-only Bcl-2 proteins so that theyare released to bind to the pro-apoptotic Bcl-2 proteins, therebytriggering the MOMP process. In short, there are two types of Bcl-2heterodimers: (1) pro-apoptotic Bcl-2 heterodimers, formed between anactivator BH3-only Bcl-2 protein and a multi-domain pro-apoptotic Bcl-2protein; and (2) anti-apoptotic Bcl-2 heterodimers, formed between amulti-domain anti-apoptotic Bcl-2 protein and an activator BH3-onlyBcl-2 protein or between a multi-domain anti-apoptotic Bcl-2 protein anda multi-domain pro-apoptotic Bcl-2 protein. Formation of pro-apoptoticBcl-2 heterodimers promote apoptosis while formation of anti-apoptoticheterodimers promote cell survival.

The presence of a particular pro- or anti-apoptotic Bcl-2 heterodimer ina patient is known to indicate that patient's responsiveness to a drugthat blocks formation of the particular heterodimer and inhibits itsfunction. See, e.g., Letai, Nature Reviews Cancer, 8:121-132 (2008). Inone example, the drug is a mimetic of BH3-only protein that competesagainst the BH3-only protein for binding to its cognate partner. Inanother example, the drug targets an upstream apoptotic factor andultimately blocks formation of a Bcl-2 heterodimer.

Many cancer drugs induce apoptosis in cancer cells by blocking formationof anti-apoptotic Bcl-2 heterodimers. The presence of a particularanti-apoptotic Bcl-2 heterodimer in a cancer patient indicates that thispatient is sensitive to a drug that interferes with formation of thisanti-apoptotic Bcl-2 heterodimer. See Deng, et al Cancer Cell12(2):171-85 (2007). On the other hand, apoptosis inhibitors are usedfor treating neurodegenerative disease or cardiovascular disease, bothof which involve apoptosis. In these cases, the presence of a particularpro-apoptotic Bcl-2 heterodimer in a neurodegenerative disease patientor a cardiovascular disease patient indicates that such a patient issensitive to an apoptosis inhibitor that blocks formation of theparticular pro-apoptotic Bcl-2 heterodimer.

Bcl-2 heterodimer profiling can also be used to predict responsivenessto drugs targeting the apoptotic pathway in patients suffering fromother apoptosis-related diseases, e.g., autoimmune disease (see Adams etal., Cold Spring Harb Symp Quant Biol. 70:469-477; 2005).

Without further elaboration, it is believed that one skilled in the artcan, based on the above description, utilize the present invention toits fullest extent. The following specific embodiments are, therefore,to be construed as merely illustrative, and not limitative of theremainder of the disclosure in any way whatsoever. All publicationscited herein are incorporated by reference.

EXAMPLE 1 Preparation of Monoclonal Antibodies Specific to Bcl-2Heterodimers

Genes encoding human Bcl-xL, Bcl-2, and Mcl-2 are cloned and mutated todelete their transmembrane domains. The mutated genes are linked to anucleotide sequence encoding glutathione-S-transferase (GST) and clonedinto pGEX 4T-1 to obtain DNA constructs for expressing Bcl-xL(Δtd)-GST,Bcl-2(Δtd)-GST, and Mcl-2(Δtd)-GST fusion proteins. DNA constructs forexpressing full length human Bax, Bak, Bak, Bim, Bid, Bad, Puma, andNoxa, all fused with GST, are prepared by recombinant technology.

All of the DNA constructs are introduced into BL2I E. coli cells.Positive transformants are cultured in a suitable medium and expressionof the fusion proteins are induced withisopropyl-1-thio-β-D-galactopyranoside. The expressed fusion proteinsare purified using Amersham Hitrap Glutathion e column on the ACTA-FPLC(Amersham) and accurately quantified using spectrophotometry.

Bcl-xL(Δtd)-GST, Bcl-2(Δtd)-GST, or Mcl-2(Δtd)-GST is mixed withBax-GST, Bak-GST, Bak-GST, Bim-GST, Bid-GST, Bad-GST, Puma-GST, orNoxa-GST at equamolar amounts in PBS. The mixture is stirred on ice for12 hours to allow formation of heterodimers.

The heterodimmers are purified using a sepharose 12 column (Pharmacia)on a ACTA-FPLC (Amersham), following the method described in Zue et al.,Protein Science 6: 781-788 (2007).

Each of the heterodimers (1 μg) is suspended in monophosphoryl lipid Aplus trehalose dicorynomycloate adjuvant (Ribi Immunochem. ResearchInc., Hamilton, Mont.). The mixture thus formed are injected into Balb/cmice at each hind foot pad once every 3-4 days for 14 times. Three daysafter the final injection, spleen cells are removed from the mice and asingle cell suspension is prepared in a DMEM medium (Gibco/BRL Corp.)supplemented with 1% penicillin-streptomycin. The spleen cells are fusedwith murine myeloma cells P3X63AgU.1 (ATCC CRL 1597) using 35%polyethylene glycol and cultured in 96-well culture plates.

Hybridomas are selected in super DMEM [DMEM supplemented with 10% fetalcalf serum FCS, 100 mM pyruvate, 100 U/ml insulin, 100 mM oxaloaceticacid 2 mM glutamine, 1% nonessential amino acids (GIBCO/BRL), 100 U/mlpenicillin, and 100 μg/ml streptomycin] containing 100 μM hypoxanthine,0.4 μM aminopterin, and 16 μM thymidine (HAT), (Sigma Chemical Co., St.Louis. Mo.).

Hybridoma cells are fed with 200 μl of super DMEM containing 10% FCS andantibiotics. Ten days after the fusion, supernatants of the hybridomacultures are collected and screened for the presence of antibodies thatbind to the cognate heterodimer protein and/or to either member of theheterodimer (as negative controls) in a capture ELISA as described inCerto et al., Cancer Cell., 9(5):351-365 (2006).

Briefly, 96-well microtiter plates (Maxisorb; Nunc, Kamstrup, Denmark)are coated with 50 μl (1 μg/ml) of a heterodimer or a member of theheterodimer at 4° C. overnight. The plates are then washed three timeswith PBS containing 0.05% TWEEN 20™ (PBST) and blocked with 50 μl PBScontaining 2.0% bovine serum albumin (BSA) at room temperature for 1hour. The plates are then washed again three times with PBST.Afterwards, 100 μl of a hybridoma supernatant is added to designatedwells. The plates are incubated at room temperature for 1 hour on ashaker apparatus and then washed three times with wash buffer. Next, 50μl HRP-conjugated goat anti-mouse IgG Fe (Cappel Laboratories), diluted1:1000 in assay buffer (0.5% bovine serum albumin, 0.05% % TWEEN 20™,0.01% Thimersol in PBS), is added to each well. The plates are thenincubated for 1 hour at room temperature on a shaker apparatus andwashed three times with wash buffer, followed by addition of 50 μl ofsubstrate DACO and incubation at room temperature for 10 minutes. 50 μldiethyl glycol were added to each well to stop the reaction andabsorbance at 450 nm in each well is read in a microtiter plate reader.

Hybridoma cells producing antibodies that bind to a heterodimer but notto either member of the heterodimer are selected. These positivehybridoma cells are cloned twice and the specificity of the antibodiesproduced thereby are retested. The isotypes of the antibodies having thedesired specificity are determined by conventional methods, e.g., usingisotype specific goat anti-mouse Igs (Fisher Biotech, Pittsburgh, Pa.).

EXAMPLE 2 Preparation of Polyclonal Antibodies Specific to Bcl-2Heterodimers

New Zealand rabbits were immunized on the back and proximal limbs of therabbits with 0.1 ml of a Bcl-2 heterodimer (50 ug/ml) prepared followingthe method described in Example 1. The heterodimer is pre-mixed with 50%Freund's complete adjuvant. The immunization is repeated 28th dayslater. On day 35, 0.5 ml of blood is obtained from each of the immunizedrabbits and antibody titers in the blood samples are determined byELISA. Anti-sera are collected from the arterial carotid of rabbitshaving high antibody titers.

The specificity of the antibodies in each antiserum is examined byconventional methods, e.g., the immunoprecipitation and FACS assaysdescribed in Examples 4 and 5 below.

EXAMPLE 3 Screening for scFv Antibodies Specific to Bcl-2 heterodimersUsing a Yeast scFv Library

A nonimmune human scFv yeast library (using expression vector pYD1) isobtained from Pacific Northwest National Laboratories(http://www.sysbio.org/dataresources/singlechain.stm). In this library,a scFv antibody, in which the heavy and light chains is connected by aflexible polypeptide linker, is fused to the adhesion subunit of theyeast agglutinin protein Aga2p and the HA-tag. Upon expression, the scFvis located on the surface of a yeast host cell via binding of Aga2P toAga1P, a cell surface protein. See FIG. 4. Each yeast cell typicallydisplays 1×10⁵ to 1×10⁶ copies of the scFv and the surface expression ofthe scFv. Variations in surface expression can be measured throughimmunofluorescence labeling of the HA-tag flanking the scFv region. SeeFIG. 4.

The scFv library described above is introduced into yeast strain EBY100(Invitrogen) and scFv antibodies having the desired specificity areidentified as follows. The EBY yeast cells are first grown overnight in1 liter of SDCAA medium (containing 20 g dextrose, 6.7 g Difco yeastnitrogen base, 5 g Bacto casamino acids, 5.4 g Na₂HPO₄ and 8.56 gNaH₂PO₄H₂O). 1×10¹⁰ yeast cells from the overnight culture areprecipitated by centrifugation at 2,500 g for 5 minutes and resuspendedin SGCAA medium (a medium identical to SDACC except that it containsgalactose instead of dextrose) to an absorbance of about 0.5-1 at 600nm. The yeast cells are then cultured at 20° C. for 36 h to allowexpression of scFv antibodies. Afterwards, the cells are collected bycentrifugation at 2,500 g for 5 min. The cell pellet is washed with 25ml PBS.

Yeast cells expressing scFv antibodies are sorted by flow cytometry.Briefly, about 1×10⁶ to 1×10⁷ yeast cells prepared as described aboveare collected via centrifugation at 14,000 g for 30 seconds, washed with1 ml PBS buffer, and mixed with 2 μl of 10 μg/ml anti-HA phycoerythrinmonoclonal antibody (SIGMA-ALDRICH) and Bcl-2/Bid heterodimer, in whichBcl-2 is labeled with FITC and Bid is labeled with Texas red. Afterbeing incubated at room temperature for 1 hour, the mixture iscentrifuged at 12,000 g for 30 seconds to precipitate yeast cells. Thecell pellet thus formed is resuspended in 500 μl 10 mM Tris (final celldensity ˜10⁶/ml) and subjected to cell sorting by flow cytometry asfollows.

A flow cytometry protocol is pre-determined using EBY100 yeast cellsmixed with the anti-HA phycoerythrin antibody as a positive control andEBY100 yeast cells mixed with the double-labeled heterodimer as anegative control. Compensation is performed to reject crosstalk betweenthe FITC, Texas red, and phycoerythrin channels of the fluorescencedetector. The labeled yeast cells are loaded into a FACSAria Cell-Sorter(Becton Dickinson, Mountain View, Calif.) and gated on forward- and sidescatter channels. An appropriate sort gate in the FITC/Texasred/phycoerythrin positive quadrant is drawn and the top 5%triple-positive yeast cells are collected in 1 ml SDCAA media. Ifnecessary, the top 0.1% triple-positive yeast cells are collected toensure that only cells having high affinity to Bcl-2/Bid heterodimer issorted.

The triple-positive cells thus identified are suspended in 10 ml SDCAAand grown over night at 30° C. These cells are then subjected to tworounds of negative selection to exclude cells expressing scFv antibodiesthat also bind to Bcl-2 or Bid monomer. More specifically, the cells areincubated with FITC-labeled Bcl-2 and Texas red-labeled Bid andfollowing the same procedure described above, FITC and Texas red doublenegative cells are sorted. The cells thus collected are labeled with thedouble-labeled Bcl-2/Bid heterodimer to confirm their binding to theheterodimer.

The yeast cell thus identified are diluted and plated to allow formationof individual clones, Plasmid DNAs are isolated from these clones usinga Zymoprep kit (Zymo Research, Orange, Calif.) as described inWeaver-Feldhaus et al., Protein Engineering, Design & Selection vol. 18,no. 11, pp 527-536 (2005). The scFv sequence included in each plasmidDNA is determined following the method described in Chao et al., NatureProtocols 1:755-768 (2006).

The scFv antibodies thus identified are analyzed by ELISA and FACS toconfirm their specificity to Bcl-2/Bid heterodimer. They can subject tomutagenesis to select for scFv antibodies having higher affinity andspecificity to Bcl-2/Bid heterodimer.

EXAMPLE 4 Select Antibodies Specific to Bcl-2 Heterodimers byImmunoprecipitation

An immunoprecipitation assay, as illustrated in FIG. 2, is performed toensure that the antibodies obtained in Example 1 above are specific toBcl-2 heterodimers. The Two members of a Bcl-2 heterodimer areconjugated with two fluorescent probes that have distinct emissionspectra, i.e., one labeled with fluorescein isothiocyanate (FITC; whichemit at 488 nm) and the other labeled with Texas red (which emits at 590nm). See FIG. XX. The labeled members are incubated together to allowformation of the Bcl-2 heterodimer, following the method described inExample 1 above. 0.1 μg of the heterodimer thus formed is incubated with50 uL of supernatant from a hybridoma clone that produces an antibody ofinterest in 0.5 mL PBS containing 0.05% tween-20. The non-dimerizedlabeled members of the heterodimer are used as negative controls. Themixtures are incubated for 1 hour on ice to allow formation ofantibody-antigen complexes and 10 ul of GammaBing-G sepharose beds (GEHealthcare Piscataway, N.Y.) are added to the mixture. After beingincubated on ice for 30 minutes on ice with rotation, the mixtures arecentrifuged at 10,000 g for 30 seconds. The pellet beads, to which theantibody-antigen complexes are attached, are washed several times andmeasured for optical density at 488 nm (OD₄₈₈) and 590 nm (OD₅₉₀). Thespecificity of the antibody is determined based on the values of OD₄₈₈and 590 nm OD₅₉₀.

EXAMPLE 5 Select Antibodies Specific to Bcl-2/Bim Heterodimer by FlowCytometry

Mitochondria from cells having a high level of Bcl2/Bim heterodimer andfrom cells having Bcl-2 knocked-out are purified and labeled asdescribed in Methods Enzymol. 2000; 322:235-42 and Cancer Cell 2004;Cell 2, 183-192. See FIG. 3, Panels A and B. Briefly, the just-mentionedtwo types of cells are suspended in cold hypotonic lysis buffer, 259 mMsucrose, 10 mM Tris-Hcl pH (7.4), 1 mM EGTA, and homogenized in a douncerotary Teflon pestle, followed by 6-10 expulsions through a 27-gaugeneedle. The fractions containing mitochondria are collected bydifferential centrifugation and resuspended in an assay binding buffer(125 mM KCL, 10 mM Tris-HCl (pH 7.4), 0.1 mM EGTA, pH 7.2, 20 uM ATP) toa final protein concentration of 5 mg/ml.

Twenty-five microliters of the suspension (4 mg of mitochondrialprotein/ml) are suspended with PBS containing 1% FCS, (FACS buffer) andmixed with 100 μl of a hybridoma culture supernatant containing a testantibody or a test antibody in purified form (purified on Protein-Gsepharose column; 10 μg/ml in the FACS buffer) in a U-bottom microtiterwells. Rhodamine-labeled polyclonal anti-VDAC-1 antibody (Merridian LifeSciences, Inc. Cincinnati, Ohio), an antibody specific to mitochondria,is also added to each well. 100 μl of fluorescein isothiocyanate(FITC)-conjugated goat anti-mouse immunoglobulin are then added to themitochondria-antibody mixture. After being incubated at 4° C. for 30min, the mixture is washed with the FACS buffer and centrifuged at 12 gfor 5 minutes to precipitate mitochondria The mitochondrial pellet isresuspended in 150 μl of FACS buffer and analyzed by FACScan (BectonDickinson, Mountain View, Calif.), with flow cytometry parameterspre-determined using control mitochondrial samples, i.e., unlabeledmitochondria as a negative control sample and anti-VDAC-1-Rhodaminelabeled mitochondria as a positive control. The mitochondrial suspensionis loaded into the flow cytometry apparatus using a FACS tube andsignals released from FITC and Rhodamine are detected. If themitochondrial suspension is double positive for both FITC and Rhodamine,it indicates that the test antibody is capable of binding to theBcl-2/Bim heterodimer. See FIG. 3, Panel A.

EXAMPLE 6 Detecting Bcl-2 Heterodimers in Fixed Cells

Cells characterized for having a prevalent Mcl-1/Bim or Bcl-2/Bidheterodimer are used in this study. See Certo et al., Cancer Cell.9(5):351-365 (2006), Moore et al., J. Clin. Invest. 117(1):112-121(2007), Deng et al., Cancer Cell. 12(2):171-185 (2007), and Letai,Nature Reviews Cancer 8:121 (2008). These cells, placed on cover slips,are fixed with 2-4% formaldehyde (Formaldehyde, 16%, methanol free,Polysciences, Inc.) in PBS for 15 minutes at room temperature. Thecell-containing cover slips are rinsed with PBS three times, 5 minutesfor each. the slips are then soaked in a blocking buffer (TBST/5% normalgoat serum: to 5 ml 1×TBST add 250 μl normal goat serum) for 60 minutes.After the blocking buffer is aspirated, an antibody specific to eitherMcl-1/Bim or Bcl-2/Bid heterodimer (0.1 to 15 mg/ml) is added to theslips. An anti-human-VDAC-1 antibody is also added to localizemitochondria. After being incubated at 4° C. overnight, the slips arerinsed three times with PBS, 5 minutes each time. Afluorochrome-conjugated secondary antibody, diluted in a dilutionbuffer, is then added. After being incubated for 1-2 hours at roomtemperature in dark, the slips are rinsed with PBS three time, 2 minuteseach time, and subsequently treated with Prolong® Gold Antifade Reagent(Invitrogen, San Diego, Calif.). The slips are then sealed by paintingaround edges of the slips with nail polish and observed under aninverted fluorescent microscope. Localization of the antibody onmitochondria indicates that the antibody recognizes Mcl-1/Bimheterodimer or Bcl-2/Bid heterodimer.

EXAMPLE 7 Detecting Bcl-2 Heterodimers in Fixed Tissue Samples

Paraffin embedded and frozen thin section tissue samples from cancerpatients and healthy subjects are purchased from Imgenex, San Diego,Calif. These samples are spotted on microarray chips (4 mm×4 mm spotsthat are 4 mm thick). The adjacent normal tissues from the samepatients/healthy subjects are also spotted on the array chips.

The microarray chips mentioned above are washed in turn with xylenethree times, 5 minutes each time, 100% ethanol twice, 10 minutes eachtime, 95% ethanol, twice, 10 minutes each time, and finally dH₂O twice,5 minutes each time. The chips are then soaked in 1 mM EDTA, pH 8.0,heated to boiling, and then kept at a sub-boiling temperature for 15minutes.

If the tissue samples on the microarray chips are fixed with formalin,the chips are washed in turn with 100%, 95%, 80% ethanol 3 times each, 3minutes each time, followed by two washes with dH₂O, 3 minutes each. Thechips are then soaked in 0.01 M sodium citrate, pH 6.0 for 20 minutes.

The chips are then washed with dH₂O three times, 5 minutes each time,incubated in 3% hydrogen peroxide for 10 minutes (this step is notneeded for formalin fixed samples), and washed again with dH₂O twice, 5minutes each time.

Next, the chips are subjected to immunostaining using the antibodiesprepared in Example 1 or an anti-VDAC1 antibody as a control. The chipsare soaked in a wash buffer for 5 minutes and then in 100-400 μl of ablocking buffer (TBST containing 5% normal goat serum) for one hour.After decanting the blocking solution, the chips are incubated with100-400 μl of an anti-Bcl-2-heterodimer antibody (primary antibody),diluted to 0.1 to 15 ug/ml for each chip, overnight at 4° C. Afterwardsthe chips are washed with the wash buffer three times, 5 minutes eachtime, and then incubated with 100-400 μl of a biotinylated goatanti-mouse Ig antibody (the secondary antibody), which is diluted inTBST following the manufacturer's protocol, for 30 minutes at roomtemperature. The chips are then washed with the wash buffer three times,5 minutes each time, and incubated with 100-400 μl ABC reagent(Vectastain ABC Kit, Vector Laboratories, Inc., Burlingame, Calif.),which is prepared following the manufacturer's instructions, for 30minutes at room temperature. After being washed for three times with thewash buffer, the chips are incubated with 100-400 μl DAB for signaldevelopment. The chips are immersed in dH₂O immediately after a colorhas developed thereon. When necessary, the chips are counterstained withhematoxylin and DAPI following manufacturer's instructions.

The stained chips are dehydrated by incubation sequentially in 95%ethanol two times, 10 seconds each, in 100% ethanol two times, 10seconds each, and finally in xylene two times, 10 seconds each. Thechips are then mounted with cover slips and examined using Fluorescenceand UV microscopy for staining patterns. The staining patterns obtainedfrom cancer tissue samples are compared with those obtained fromadjacent normal tissues.

EXAMPLE 8 Profiling Bcl-2 Heterodimers on Mitochondria Using Color CodedMicro-Beads

As shown in FIG. 5, micro-beads of 5 micron diameter and color coded(Luminex Incorporated) are derivatized with an anti-human VDAC-1antibody, which recognizes mitochondria. Mitochondrial samples preparedby different patients, as described above, are incubated with differentcolored VDAC derivatized Luminex beads and fluorescent probe-labeledantibodies specific to Bcl-2 heterodimers, as prepared by the methoddescribed in Example 1. The labeling pattern (i.e., color combination)of each mitochondrial sample is examined by conventional methods and theBcl-2 heterodimer profile of each patient is determined based on thelabeling patter. This profile can be used to diagnose certain diseaseindications and chemsensitivities, as well as predict outcomes oftreatment for cancer or other diseases associated with apoptosis.

OTHER EMBODIMENTS

All of the features disclosed in this specification may be combined inany combination. Each feature disclosed in this specification may bereplaced by an alternative feature serving the same, equivalent, orsimilar purpose. Thus, unless expressly stated otherwise, each featuredisclosed is only an example of a generic series of equivalent orsimilar features.

From the above description, on skilled in the art can easily ascertainthe essential characteristics of the present invention, and withoutdeparting from the spirit and scope thereof, can make various changesand modifications of the invention to adapt it to various usages andconditions. Thus, other embodiments are also within the claims.

1-9. (canceled)
 10. A method for detecting the presence of a heterodimerof the Bcl-2 family in a fixed tissue sample, comprising (a) contactingan isolated antibody specifically binding to a heterodimer selected fromBim and Mcl-1, Bim and Bcl-2, and Bid and Bcl-2 to a fixed tissue samplesuspected of having a heterodimer of the Bcl-2 family; (b) detecting asignal that indicates binding of the antibody to the heterodimer, and(c) determining the presence of the heterodimer in the fixed tissuesample based on the intensity of the signal. 11-12. (canceled)
 13. Themethod of claim 10, wherein the fixed tissue sample is a peripheralblood sample, a lymph-node sample, a bone marrow sample, or an organtissue sample.
 14. The method of claim 10, wherein the fixed tissuesample is a mitochondrial fraction. 15-21. (canceled)
 22. The method ofclaim 10, wherein the fixed tissue sample is a paraffin embedded tissuesample.
 23. The method of claim 10, wherein the fixed tissue sample is afrozen thin section tissue sample.